Serves as an individual contributor responsible for project management of key Clinical Supply Chain documentation, tasks and simple packaging activities in a GMP environment.

Responsibilities

• Planning, scheduling, coordination and execution, in support of CSPMs to ensure the timely availability of investigational drug supplies and related services to clinical sites and depots.
• Translates stability and packaging requests into an executed packaging design.
• Identifies, develops, communicates and tracks task completion dates , activities, logistics, and milestones in support of CSPMs to ensure the  timely availability of investigational drug supplies .
• Responsible for creating appropriate protocol specific manufacturing and packaging work orders in concert with the CSPM.
• Responsible to complete, upon request of the CSPM, tasks identified for the Center of Excellence team.

Key Stakeholders:

• The Clinical Drug Supply Chain including R43E, Analytical, Quality, and globally with our Germany counterparts as this role is key in the transfer of clinical drug to Germany from Lake County.